Evidence map›Paper›PMID 33933406›Full record

ArticleJACC. Clinical electrophysiology2021

Self-Similar Synchronization of Calcium and Membrane Potential Transitions During Action Potential Cycles Predict Heart Rate Across Species.

Syevda Tagirova Sirenko, Kenta Tsutsui, Kirill V Tarasov, Dongmei Yang, Ashley N Wirth, Victor A Maltsev, Bruce D Ziman, Yael Yaniv, Edward G Lakatta

Open access · greenAbstract read
In one paragraph

Article in JACC. Clinical electrophysiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 28% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. What makes the sinoatrial node tick? A question not for the faint of heart.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2023
    Review
  8. Article
  9. Article
  10. Heart Rate, Hibernation, and the Power Law.JACC. Clinical electrophysiology · 2021
    Article
  11. Article
  12. CaFrontiers in physiology · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 3 countries.

Syevda Tagirova SirenkoLaboratory of Cardiovascular Science, National Institute on Aging, National Institute of Health, Baltimore, Maryland, USA. Electronic address: tagirovas@mail.nih.gov.
Kenta TsutsuiLaboratory of Cardiovascular Science, National Institute on Aging, National Institute of Health, Baltimore, Maryland, USA; Saitama International Medical Center, Saitama, Japan.
Kirill V TarasovLaboratory of Cardiovascular Science, National Institute on Aging, National Institute of Health, Baltimore, Maryland, USA.
Dongmei YangLaboratory of Cardiovascular Science, National Institute on Aging, National Institute of Health, Baltimore, Maryland, USA.
Ashley N WirthLaboratory of Cardiovascular Science, National Institute on Aging, National Institute of Health, Baltimore, Maryland, USA.
Victor A MaltsevLaboratory of Cardiovascular Science, National Institute on Aging, National Institute of Health, Baltimore, Maryland, USA.
Bruce D ZimanLaboratory of Cardiovascular Science, National Institute on Aging, National Institute of Health, Baltimore, Maryland, USA.
Yael YanivBiomedical Engineering Faculty, Technion-IIT, Haifa, Israel.
Edward G LakattaLaboratory of Cardiovascular Science, National Institute on Aging, National Institute of Health, Baltimore, Maryland, USA. Electronic address: LakattaE@mail.nih.gov.
National Institute on Aging · USSaitama International Medical Center · JPTechnion – Israel Institute of Technology · IL

Funding

Beat to beat Ca2+-dependent regulation of pacemaker cell rate and rhythmZIAAG000598 · NIA · NATIONAL INSTITUTE ON AGING · PI LAKATTA, EDWARD · 2011 to 2025
$3.5M
Intramural NIH HHS Z99 AG999999
6 · The paper itself

Abstract

objectivesThe purpose of this study was to discover regulatory universal mechanisms of normal automaticity in sinoatrial nodal (SAN) pacemaker cells that are self-similar across species.

backgroundTranslation of knowledge of SAN automaticity gleaned from animal studies to human dysrhythmias (e.g., "sick sinus" syndrome [SSS]) requiring electronic pacemaker insertion has been suboptimal, largely because heart rate varies widely across species.

methodsSubcellular Ca

resultsAlthough both AP cycle lengths (APCLs) and Ca

conclusionsIn designing optimal heart rate to match widely different BM and energy requirements from mice to humans, nature did not "reinvent pacemaker cell wheels," but differentially scaled kinetics of gears that regulate the rates at which the "wheels spin." This discovery will facilitate the development of novel pharmacological and biological pacemakers featuring a normal, wide-range rate regulation in animal models and the translation of these to humans to target recalcitrant human SSS.

Indexed as

CalciumSinoatrial NodeAction PotentialsAnimalsGuinea PigsHeart RateMembrane PotentialsMiceRabbitsCalciumaction potentialsCa(2+) and Vm kinetic transitionscardiac pacemaker cellsheart ratelong-range power law correlationssubcellular local Ca(2+) releases

Identifiers

PMID33933406
PMCPMC10089231
OpenAlexW3157637735

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.